Rabson-Mendenhall Syndrome: A Case Report
نویسندگان
1 MD,Assistant Professor of Pediatric Endocrinology, Shahid Beheshti University of Medical Sciences,Tehran,Iran
2 MD,Ph.D,Assistant Professor of Pediatric Rheumatology,Shahid Beheshti University of Medical Sciences,Tehran,Iran
3 MD, Resident of Pediatric ,Shahid Beheshti University of Medical Sciences, Tehran,Iran
doi
10.22037/ijcn.v4i1.1726چکیده
Rabson-Mendenhall syndrome is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, paradoxical fasting hypoglycemia, postprandial hyperglycemia, extreme hyperinsulinemia and pineal hyperplasia. Herein, we described a 10- year-old girl with physical features of the Rabson-Mendenhall syndrome that was presented with polyuria. To our knowledge, this is the first report of the Rabson-Mendenhall syndrome from Iran.
